Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study

被引:21
|
作者
Dixon-Suen, Suzanne C. [1 ]
Lewis, Sarah J. [2 ,3 ]
Martin, Richard M. [2 ,3 ,4 ,5 ]
English, Dallas R. [1 ,6 ]
Boyle, Terry [7 ,8 ]
Giles, Graham G. [1 ,6 ,9 ]
Michailidou, Kyriaki [10 ,11 ]
Bolla, Manjeet K. [12 ]
Wang, Qin [12 ]
Dennis, Joe [12 ]
Lush, Michael [12 ]
Ahearn, Thomas U. [14 ]
Ambrosone, Christine B. [15 ]
Andrulis, Irene L. [16 ,17 ]
Anton-Culver, Hoda [18 ]
Arndt, Volker [19 ]
Aronson, Kristan J. [20 ,21 ]
Augustinsson, Annelie [22 ]
Auvinen, Paivi [23 ,24 ]
Beane Freeman, Laura E. [14 ]
Becher, Heiko [25 ]
Beckmann, Matthias W. [26 ]
Behrens, Sabine [27 ]
Bermisheva, Marina [28 ]
Blomqvist, Carl [29 ,30 ]
Bogdanova, Natalia, V [31 ,32 ]
Bojesen, Stig E. [33 ,34 ]
Bonanni, Bernardo [35 ]
Brenner, Hermann [19 ,36 ,37 ]
Bruening, Thomas [38 ]
Buys, Saundra S. [39 ,40 ]
Camp, Nicola J. [39 ,40 ]
Campa, Daniele [27 ,41 ]
Canzian, Federico [42 ]
Castelao, Jose E. [43 ]
Cessna, Melissa H. [44 ,45 ]
Chang-Claude, Jenny [27 ,46 ]
Chanock, Stephen J. [14 ]
Clarke, Christine L. [47 ]
Conroy, Don M. [48 ]
Couch, Fergus J. [49 ]
Cox, Angela [50 ]
Cross, Simon S. [51 ]
Czene, Kamila [52 ]
Daly, Mary B. [53 ]
Devilee, Peter [54 ,55 ]
Doerk, Thilo [32 ]
Dwek, Miriam [56 ]
Eccles, Diana M. [57 ]
Eliassen, A. Heather [58 ,59 ,60 ]
机构
[1] Canc Council Victoria, Canc Epidemiol Div, Melbourne, Vic, Australia
[2] Univ Bristol, Bristol Med Sch, Dept Populat Hlth Sci, Bristol, Avon, England
[3] Univ Bristol, MRC, Integrat Epidemiol Unit, Bristol, Avon, England
[4] Univ Hosp Bristol & Weston NHS Fdn Trust, NIHR Biomed Res Ctr, Bristol, Avon, England
[5] Univ Bristol, Bristol, Avon, England
[6] Univ Melbourne, Melbourne Sch Populat & Global Hlth, Ctr Epidemiol & Biostat, Melbourne, Vic, Australia
[7] Univ South Australia, Allied Hlth & Human Performance, Adelaide, SA, Australia
[8] Univ South Australia, Canc Res Inst, Australian Ctr Precis Hlth, Adelaide, SA, Australia
[9] Monash Univ, Sch Clin Sci Monash Hlth, Precis Med, Clayton, Vic, Australia
[10] Cyprus Inst Neurol & Genet, Biostat Unit, Nicosia, Cyprus
[11] Cyprus Inst Neurol & Genet, Cyprus Sch Mol Med, Nicosia, Cyprus
[12] Univ Cambridge, Ctr Canc Genet Epidemiol, Dept Publ Hlth & Primary Care, Cambridge, England
[13] Univ Sydney, Australian Breast Canc Tissue Bank, Westmead Inst Med Res, Sydney, NSW, Australia
[14] NCI, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
[15] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
[16] Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Fred A Litwin Ctr Canc Genet, Toronto, ON, Canada
[17] Univ Toronto, Dept Mol Genet, Toronto, ON, Canada
[18] Univ Calif Irvine, Dept Med, Genet Epidemiol Res Inst, Irvine, CA 92717 USA
[19] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Heidelberg, Germany
[20] Queens Univ, Dept Publ Hlth Sci, Kingston, ON, Canada
[21] Queens Univ, Canc Res Inst, Kingston, ON, Canada
[22] Lund Univ, Dept Canc Epidemiol, Clin Sci, Lund, Sweden
[23] Kuopio Univ Hosp, Canc Ctr, Dept Oncol, Kuopio, Finland
[24] Univ Eastern Finland, Inst Clin Med, Oncol, Kuopio, Finland
[25] Univ Med Ctr Hamburg Eppendorf, Inst Med Biometry & Epidemiol, Hamburg, Germany
[26] Friedrich Alexander Univ Erlangen Nuremberg, Univ Hosp Erlangen, Comprehens Canc Ctr, ER,EMN,Dept Gynecol & Obstet, Erlangen, Germany
[27] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[28] Russian Acad Sci, FSBSI Ufa Fed Res Ctr, Inst Biochem & Genet, Ufa, Russia
[29] Univ Helsinki, Helsinki Univ Hosp, Dept Oncol, Helsinki, Finland
[30] Orebro Univ Hosp, Dept Oncol, Orebro, Sweden
[31] Hannover Med Sch, Dept Radiat Oncol, Hannover, Germany
[32] Hannover Med Sch, Gynaecol Res Unit, Hannover, Germany
[33] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Copenhagen Gen Populat Study, Herlev, Denmark
[34] Copenhagen Univ Hosp, Herlev & Gentofte Hosp, Dept Clin Biochem, Herlev, Denmark
[35] European Inst Oncol IRCCS, Div Canc Prevent & Genet, Milan, Italy
[36] German Canc Res Ctr, Div Prevent Oncol, Heidelberg, Germany
[37] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[38] Inst Ruhr Univ Bochum, German Social Accid Insurance IPA, Inst Prevent & Occupat Med, Bochum, Germany
[39] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA
[40] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[41] Univ Pisa, Dept Biol, Pisa, Italy
[42] German Canc Res Ctr, Genom Epidemiol Grp, Heidelberg, Germany
[43] Inst Invest Sanitaria Galicia Sur IISGS, Xerencia Xest Integrada Vigo SERGAS, Oncol & Genet Unit, Vigo, Spain
[44] Intermt Healthcare, Intermt Med Ctr, Dept Pathol, Salt Lake City, UT USA
[45] Intermt Healthcare, Intermt Biorepository, Salt Lake City, UT USA
[46] Univ Med Ctr Hamburg Eppendorf, Univ Canc Ctr Hamburg UCCH, Canc Epidemiol Grp, Hamburg, Germany
[47] Univ Sydney, Westmead Inst Med Res, Sydney, NSW, Australia
[48] Univ Cambridge, Ctr Canc Genet Epidemiol, Dept Oncol, Cambridge, England
[49] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[50] Univ Sheffield, Sheffield Inst Nucle Acids SInFoNiA, Dept Oncol & Metab, Sheffield, S Yorkshire, England
基金
加拿大健康研究院; 美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金; 俄罗斯基础研究基金会; 瑞典研究理事会;
关键词
GENETIC-VARIANTS; CAUSAL INFERENCE; INSTRUMENTS;
D O I
10.1136/bjsports-2021-105132
中图分类号
G8 [体育];
学科分类号
04 ; 0403 ;
摘要
Objectives Physical inactivity and sedentary behaviour are associated with higher breast cancer risk in observational studies, but ascribing causality is difficult. Mendelian randomisation (MR) assesses causality by simulating randomised trial groups using genotype. We assessed whether lifelong physical activity or sedentary time, assessed using genotype, may be causally associated with breast cancer risk overall, pre/post-menopause, and by case-groups defined by tumour characteristics. Methods We performed two-sample inverse-variance-weighted MR using individual-level Breast Cancer Association Consortium case-control data from 130 957 European-ancestry women (69 838 invasive cases), and published UK Biobank data (n=91 105-377 234). Genetic instruments were single nucleotide polymorphisms (SNPs) associated in UK Biobank with wrist-worn accelerometer-measured overall physical activity (n(snps)=5) or sedentary time (n(snps)=6), or accelerometer-measured (n(snps)=1) or self-reported (n(snps)=5) vigorous physical activity. Results Greater genetically-predicted overall activity was associated with lower breast cancer overall risk (OR=0.59; 95% confidence interval (CI) 0.42 to 0.83 per-standard deviation (SD;similar to 8 milligravities acceleration)) and for most case-groups. Genetically-predicted vigorous activity was associated with lower risk of pre/perimenopausal breast cancer (OR=0.62; 95% CI 0.45 to 0.87,>= 3 vs. 0 self-reported days/week), with consistent estimates for most case-groups. Greater genetically-predicted sedentary time was associated with higher hormone-receptor-negative tumour risk (OR=1.77; 95% CI 1.07 to 2.92 per-SD (similar to 7% time spent sedentary)), with elevated estimates for most case-groups. Results were robust to sensitivity analyses examining pleiotropy (including weighted-median-MR, MR-Egger). Conclusion Our study provides strong evidence that greater overall physical activity, greater vigorous activity, and lower sedentary time are likely to reduce breast cancer risk. More widespread adoption of active lifestyles may reduce the burden from the most common cancer in women.
引用
收藏
页码:1157 / 1170
页数:14
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